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Metolazone

NDC 0185-0055 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA076466
Dosage form / routeTABLET · ORAL
Active ingredientsMETOLAZONE (5 mg/1)
Marketing started20031219
Package count2

External sources

Source: openFDA. Public-domain (CC0).